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Vol. 286, Issue 2, 670-675, August 1998
Sanofi Recherche, Haemobiology Research Department, Toulouse,
France
SR 121566, a novel nonpeptide antiplatelet agent with high affinity and
specificity for the GP IIb/IIIa complex, exhibits potent in
vitro antiaggregating activity in rabbit platelets. This paper
reports results from a study in rabbits about the efficacy and
tolerability of SR 121787, the prodrug of SR 121566. After p.o.
pretreatment with SR 121787, ADP-, arachidonic acid- and collagen-induced rabbit platelet aggregation was inhibited ex vivo in a dose-dependent manner (ED50 between 2.3 and
6.1 mg/kg). Collagen-induced thrombocytopenia was totally abolished by
SR 121787 at 20 mg/kg p.o. In a carotid artery lesion model of arterial thrombosis, p.o. administration of SR 121787 resulted in a
dose-dependent inhibition of thrombosis with a maximum effect of 68%
(ED50 = 16.0 ± 0.3 mg/kg). Recombinant tissue
plasminogen activator-induced thrombolysis of a preformed thrombus in
the jugular vein was potentiated by SR 121787 at doses between 1 and 6 mg/kg i.v. In an ear incision bleeding model, SR 121787 at doses up to
15 mg/kg p.o. did not cause an increase in blood loss. These results
demonstrate that SR 121787 exerts oral antiplatelet, antithrombotic and
thrombolysis-enhancing efficacy in rabbits. SR 121787 appears to be a
promising compound for evaluation under clinical conditions in the
therapy of acute coronary syndromes.